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儿科急性呼吸窘迫综合征的发病率和流行病学(PARDIE):一项国际性、观察性研究。

Paediatric acute respiratory distress syndrome incidence and epidemiology (PARDIE): an international, observational study.

机构信息

Department of Anesthesiology and Critical Care Medicine, Children's Hospital Los Angeles, Los Angeles, CA, USA; Department of Pediatrics, University of Southern California Keck School of Medicine, Los Angeles, CA, USA.

University of Washington, Seattle Children's Hospital, Seattle, WA, USA.

出版信息

Lancet Respir Med. 2019 Feb;7(2):115-128. doi: 10.1016/S2213-2600(18)30344-8. Epub 2018 Oct 22.

Abstract

BACKGROUND

Paediatric acute respiratory distress syndrome (PARDS) is associated with high mortality in children, but until recently no paediatric-specific diagnostic criteria existed. The Pediatric Acute Lung Injury Consensus Conference (PALICC) definition was developed to overcome limitations of the Berlin definition, which was designed and validated for adults. We aimed to determine the incidence and outcomes of children who meet the PALICC definition of PARDS.

METHODS

In this international, prospective, cross-sectional, observational study, 145 paediatric intensive care units (PICUs) from 27 countries were recruited, and over a continuous 5 day period across 10 weeks all patients were screened for enrolment. Patients were included if they had a new diagnosis of PARDS that met PALICC criteria during the study week. Exclusion criteria included meeting PARDS criteria more than 24 h before screening, cyanotic heart disease, active perinatal lung disease, and preparation or recovery from a cardiac intervention. Data were collected on the PICU characteristics, patient demographics, and elements of PARDS (ie, PARDS risk factors, hypoxaemia severity metrics, type of ventilation), comorbidities, chest imaging, arterial blood gas measurements, and pulse oximetry. The primary outcome was PICU mortality. Secondary outcomes included 90 day mortality, duration of invasive mechanical and non-invasive ventilation, and cause of death.

FINDINGS

Between May 9, 2016, and June 16, 2017, during the 10 study weeks, 23 280 patients were admitted to participating PICUs, of whom 744 (3·2%) were identified as having PARDS. 95% (708 of 744) of patients had complete data for analysis, with 17% (121 of 708; 95% CI 14-20) mortality, whereas only 32% (230 of 708) of patients met Berlin criteria with 27% (61 of 230) mortality. Based on hypoxaemia severity at PARDS diagnosis, mortality was similar among those who were non-invasively ventilated and with mild or moderate PARDS (10-15%), but higher for those with severe PARDS (33% [54 of 165; 95% CI 26-41]). 50% (80 of 160) of non-invasively ventilated patients with PARDS were subsequently intubated, with 25% (20 of 80; 95% CI 16-36) mortality. By use of PALICC PARDS definition, severity of PARDS at 6 h after initial diagnosis (area under the curve [AUC] 0·69, 95% CI 0·62-0·76) discriminates PICU mortality better than severity at PARDS diagnosis (AUC 0·64, 0·58-0·71), and outperforms Berlin severity groups at 6 h (0·64, 0·58-0·70; p=0·01).

INTERPRETATION

The PALICC definition identified more children as having PARDS than the Berlin definition, and PALICC PARDS severity groupings improved the stratification of mortality risk, particularly when applied 6 h after PARDS diagnosis. The PALICC PARDS framework should be considered for use in future epidemiological and therapeutic research among children with PARDS.

FUNDING

University of Southern California Clinical Translational Science Institute, Sainte Justine Children's Hospital, University of Montreal, Canada, Réseau en Santé Respiratoire du Fonds de Recherche Quebec-Santé, and Children's Hospital Los Angeles, Department of Anesthesiology and Critical Care Medicine.

摘要

背景

儿科急性呼吸窘迫综合征(PARDS)与儿童死亡率高有关,但直到最近才存在儿科专用的诊断标准。儿科急性肺损伤共识会议(PALICC)的定义是为了克服柏林定义的局限性而制定的,该定义是为成人设计和验证的。我们旨在确定符合 PALICC PARDS 定义的 PARDS 患儿的发病率和结局。

方法

在这项国际、前瞻性、横断面、观察性研究中,来自 27 个国家的 145 个儿科重症监护病房(PICU)参与了研究,在 10 周的连续 5 天时间里,所有患者都进行了筛查以确定是否符合入组条件。如果患者在研究周内新诊断为符合 PALICC 标准的 PARDS,则纳入研究。排除标准包括在筛查前 24 小时以上符合 PARDS 标准、紫绀性心脏病、活跃的围产期肺疾病、以及心脏干预的准备或恢复。收集 PICU 特征、患者人口统计学特征以及 PARDS 要素(即 PARDS 危险因素、低氧血症严重程度指标、通气类型)、合并症、胸部影像学、动脉血气测量和脉搏血氧饱和度的数据。主要结局是 PICU 死亡率。次要结局包括 90 天死亡率、有创机械通气和无创通气的持续时间以及死亡原因。

结果

在 2016 年 5 月 9 日至 2017 年 6 月 16 日的 10 个研究周期间,共有 23280 名患者入住参与研究的 PICU,其中 744 名(3.2%)被诊断为 PARDS。95%(708 例/744 例)的患者有完整的数据进行分析,死亡率为 17%(121 例/708 例;95%CI 14-20),而仅 32%(230 例/708 例)的患者符合柏林标准,死亡率为 27%(61 例/230 例)。根据 PARDS 诊断时的低氧血症严重程度,非侵入性通气且轻度或中度 PARDS 患者的死亡率相似(10-15%),但严重 PARDS 患者的死亡率较高(33%[54 例/165 例;95%CI 26-41])。160 例非侵入性通气的 PARDS 患者中有 50%(80 例)随后被气管插管,其中 25%(20 例/80 例;95%CI 16-36)死亡。使用 PALICC PARDS 定义,PARDS 诊断后 6 小时的 PARDS 严重程度(曲线下面积[AUC]0.69,95%CI 0.62-0.76)比 PARDS 诊断时的严重程度(AUC 0.64,0.58-0.71)更好地预测 PICU 死亡率,并且优于 6 小时时的柏林严重程度组(AUC 0.64,0.58-0.70;p=0.01)。

结论

PALICC 定义比柏林定义识别出更多患有 PARDS 的儿童,并且 PALICC PARDS 严重程度分组改善了死亡率风险的分层,尤其是在 PARDS 诊断后 6 小时应用时。PALICC PARDS 框架应考虑用于未来儿童 PARDS 的流行病学和治疗研究。

资金

南加州大学临床转化科学研究所、蒙特利尔圣母大学、加拿大魁北克健康研究基金会呼吸网络和洛杉矶儿童医院麻醉和危重病医学科。

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